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Eosinophilic granulomatosis with polyangiitis
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Medical condition
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Wikipedia

Eosinophilic granulomatosis with polyangiitis (EGPA), formerly known as allergic granulomatosis, is an extremely rare autoimmune condition that causes inflammation of small and medium-sized blood vessels (vasculitis) in persons with a history of airway allergic hypersensitivity (atopy).

Instance of
designated intractable/rare disease
class of disease
Subclass of
Vasculitis
anti-neutrophil cytoplasmic antibody-associated vasculitis
secondary glomerular disease
systemic inflammatory disease associated with an acquired peripheral neuropathy
Disease
References
Wikidata